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Effect of sesamin supplementation in diabetic patient

Effect of sesamin supplementation on the glycemic indices, lipid profile, serum levels of inflammatory markers, malondialdehyde and adiponectin in type2 diabetic patients.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014061818134N1
Enrollment
44
Registered
2014-11-23
Start date
2013-12-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

type 2 diabetes. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Intervention group: Sesamine supplement, 200 mg caps per day for 8 weeks. Intervention 2: Placebo group: placebo caps for 6 weeks.
Treatment - Drugs
Intervention group: Sesamine supplement, 200 mg caps per day for 8 weeks

Sponsors

Vice chancellor for research, Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Main inclusion criteria: : having type 2 diabetes; 30 to 60 years old; BMI<30; Not having severe cardiovascular, hepatic, kidney, gastrointestinal, thyroid or inflammatory diseases; Not using insulin or taking corticosteroids, NSAIDS, immunosuppressives, multivitamin-mineral, fiber and omega 3 supplements since 3 weeks prior to the study and during intervention period; No smoking or addiction; No pregnancy or lactation; Not having any weight loose or weight gain regimes; No use of antibiotics. Main exclusion criteria: drug type and dose fluctuation during intervention period; unwilling to continue the study; looking sensitivity or allergy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fasting Blood Sugar. Timepoint: Befor and after 8 weeks. Method of measurement: spectrophotometry.;Hemoglobin A1c. Timepoint: Before and after 8 weeks. Method of measurement: Chromatography.;Total Cholesterol. Timepoint: Befor and after 8 weeks. Method of measurement: spectrophotometry.;Triglyceride. Timepoint: Befor and after 8 weeks. Method of measurement: spectrophotometry.;HDL.c. Timepoint: Befor and after 8 weeks. Method of measurement: spectrophotometry.;LDL.c. Timepoint: Befor and after 8 weeks. Method of measurement: spectrophotometry.;Hs-CRP. Timepoint: Befor and after 8 weeks. Method of measurement: ELISA.;TNF-a. Timepoint: Befor and after 8 weeks. Method of measurement: ELISA.;IL-6. Timepoint: Befor and after 8 weeks. Method of measurement: ELISA.;Adiponectin. Timepoint: Befor and after 8 weeks. Method of measurement: ELISA.;Malondialdehyde. Timepoint: Befor and after 8 weeks. Method of measurement: TBARS.;Dietary Factors. Timepoint: Befor and after 8 weeks. Method of measurement: 24h recall.;Insulin. Timepoint: Befor and after 8 weeks. Method of measurement: ELISA.;Blood Pressure. Timepoint: before and after intervention. Method of measurement: Medical mercury sphygmomanometer.

Secondary

MeasureTime frame
Body weight. Timepoint: Before and after 8 weeks. Method of measurement: scale.;Waist circumference. Timepoint: Before and after 8 weeks. Method of measurement: meter.;Hip circumference. Timepoint: Before and after 8 weeks. Method of measurement: meter.;Body adiposity index. Timepoint: Before and after 8 weeks. Method of measurement: Hip circumference (cm)/height (m)1.5 – 18.;Body fat%. Timepoint: Before and after 8 weeks. Method of measurement: omron.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrnoush Zakerzadeh

School of Paramedicine, Ahvaz Jondishapur University Of Medical Sciences

zakerzadeh.m@ajums.ac.ir mehr.zakerzadeh@yahoo.com+98 61 3333 7079

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026